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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709897Generated: October 30, 2026

Potassium Iodide → alpha,alpha-Bis(4-fluorophenyl)-1-[3-(4-methylphenoxy)propyl]-4-piperidinemethanol fumarate

https://huagongshe.com/reaction/1709897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
ReactantFumaric AcidHCID 444972—
ReactantBis(4-fluorophenyl)(piperidin-4-yl)methanolHCID 11208889—
Reactant1-(3-Chloropropoxy)-4-methylbenzeneHCID 12685611—
Reactant4-(Diphenylmethylene)-1-(3-phenoxypropyl)piperidine oxalateHCID 23036335—
Solvent1-ButanolHCID 263—
Productalpha,alpha-Bis(4-fluorophenyl)-1-[3-(4-methylphenoxy)propyl]-4-piperidinemethanol fumarateHCID 2303631056%

Reaction Steps

This compound was prepared according to the procedure used to synthesize the compound of Example 1. A mixture of 3.0 g (0.01 mole) of α,α-bis (p-fluorophenyl)-4-piperidinemethanol, 1.8 g (0.01 mole) of 1-chloro-3-(4-methylphenoxy) propane, 5.3 g (0.035 mole) of anhydrous sodium carbonate and 0.3 g of potassium iodide in 100 ml of 1-butanol gave a gum as residue. The gum was purified by column chromatography on 100 g of Florisil®. Fractions eluted with 10% acetone in benzene were combined and concentrated to give a gum. This gum was converted to the fumaric acid salt and the solid was recrystallized from absolute ethanol to yield 3.2 g (56%) of title compound as a white solid, mp 193°-194° C. with decomposition. pe f 49495948.hsc

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04950674
Source datasetuspto-grants-1990_08
ORD IDord-24ade4ff58564bfd9d5cfa14ac7b0472
Source noteuspto-grants-1990_08